ZipRecruiter

Log In

1

Associate Director Clinical Data Management Jobs in Reston, VA

Inova

Director, Clinical Nutrition

Falls Church, VA · On-site

$118K - $192K/yr

... data and information to continuously improve care/practice and enhance outcomes. The Director ... Develops goals and manages fiscal department activities while ensuring compliance to all ...

Axle

Associate Director of AI and Data

Rockville, MD · On-site

... saving clinical research. Sitting at the nexus of our Data Science and Biomedical Research ... This is not merely a management role; it is a mission-critical position for a leader who is ...

Inova

Director, Clinical Nutrition

Falls Church, VA · On-site

$85K - $116K/yr

... data and information to continuously improve care/practice and enhance outcomes. The Director ... Develops goals and manages fiscal department activities while ensuring compliance to all ...

previous page

Showing results 41-60

All JobsAssociate Clinical Data Management JobsAssociate Director Clinical Data Management JobsAssociate Director Clinical Data Management Jobs in Reston, VA

Associate Director Clinical Data Management information

See Reston, VA salary details

$14

$40

$90

How much do associate director clinical data management jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for associate director clinical data management in Reston, VA is $40.52, according to ZipRecruiter salary data. Most workers in this role earn between $30.53 and $40.53 per hour, depending on experience, location, and employer.

What is an associate director clinical data management?

An Associate Director of Clinical Data Management is a senior professional responsible for overseeing the planning, execution, and management of data collected in clinical trials within the pharmaceutical or biotechnology industry. They ensure that all clinical data is accurate, secure, and compliant with regulatory standards. This role typically involves leading teams, developing data management strategies, collaborating with cross-functional departments, and ensuring that projects are delivered on time and within budget. Associate Directors also play a key role in establishing best practices and continuous process improvements within the data management function.

What are the key skills and qualifications needed to thrive as an associate director clinical data management, and why are they important?

To thrive as an Associate Director Clinical Data Management, you need a strong background in clinical research, data management, and regulatory compliance, typically supported by a life sciences degree and several years of experience in clinical data management. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and industry standards such as CDISC or GCP is crucial, with certifications like CCDM being advantageous. Leadership, strategic thinking, and excellent communication skills help drive cross-functional teams and ensure accurate data delivery. These competencies are vital because they ensure high-quality, compliant data management that supports successful clinical trials and regulatory submissions.

What are some common challenges faced by an associate director clinical data management, and how can they be addressed?

Associate Directors in Clinical Data Management often encounter challenges such as maintaining data quality across multiple studies, managing tight timelines, and ensuring compliance with evolving regulatory requirements. To address these, they implement robust data review processes, foster close collaboration between cross-functional teams (like biostatistics, clinical operations, and IT), and promote continuous training for their teams. Strong leadership and effective communication are key to navigating these challenges while delivering high-quality data for clinical trials.

What is the difference between Associate Director Clinical Data Management vs Clinical Data Manager?

AspectAssociate Director Clinical Data ManagementClinical Data Manager
ResponsibilitiesOversees data management teams, develops strategies, ensures data quality and complianceManages data collection, validation, and database setup for clinical trials
Required CredentialsBachelor's/Master's in life sciences, experience in data management, leadership skillsBachelor's in life sciences, experience in clinical data handling, technical skills
Work EnvironmentSenior-level, strategic, often in larger organizations or departmentsOperational, hands-on, often in CROs or pharmaceutical companies

The Associate Director Clinical Data Management typically holds a higher strategic role, overseeing teams and ensuring data quality across projects, while the Clinical Data Manager focuses on day-to-day data handling tasks. Both roles require similar educational backgrounds and technical skills, but differ in scope and level of responsibility.

What are popular job titles related to Associate Director Clinical Data Management jobs in Reston, VA?

For Associate Director Clinical Data Management jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Associate Director Clinical Data Management jobs in Reston, VA look for?

The top searched job categories for Associate Director Clinical Data Management jobs in Reston, VA are:

What cities near Reston, VA are hiring for Associate Director Clinical Data Management jobs?

Cities near Reston, VA with the most Associate Director Clinical Data Management job openings:

Associate Director Clinical Data Management jobs near you
Infographic showing various Associate Director Clinical Data Management job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $84,290 per year, or $40.5 per hour.

Clinical Regulatory Writer, Associate Director / Manager

AstraZeneca

Gaithersburg, MD • On-site

$133K - $199K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Job Title: Clinical Regulatory Writer, Associate Director / Manager

Location: Boston, MA OR Gaithesrburg, MD- Hybrid (3 days onsite)

Introduction to role:
Are you ready to be part of the solution, turning drug development strategies into reality? As an Associate Director in Clinical Regulatory Writing, you'll play a pivotal role in translating life-changing science into medicines. Our team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. We support AstraZeneca's core therapeutic areas across all phases of clinical development, striving for excellence in communication to achieve successful submissions and approvals.

Accountabilities:

As a Clinical Regulatory Writer, Associate Director, you will:

  • Independently manage clinical regulatory writing activities across a complex portfolio of work.

  • Author the most complex clinical-regulatory documents within a program, ensuring regulatory, technical, and quality standards are met.

  • Provide strategic communications leadership to projects, establishing communication standards and advocating for quality and efficiency.

  • Drive the development of the clinical Submission Communication Strategy (cSCS) when acting as a submission lead.

  • Lead internal/external authoring teams and partner with vendor medical writers to ensure timely and quality delivery.

  • Interpret complex data and information, condensing it into clear, concise messages that meet customer information requirements.

  • Demonstrate strategic thinking and review capabilities.

  • Collaborate proactively with other functions at the program level.

  • Support the development of Clinical Regulatory Writing Managers.

  • Drive continuous improvement and operational excellence from a communications leadership perspective.
    Essential Skills/Experience:

  • Education/Experience required:
    Associate Director level : BS Life Sciences degree or simiilar, 7+ yrs medical writing experience in pharmaceutical industry or CRO. Manager level: BS Life Sciences degree or simiilar, 2-7+ yrs medical writing experience in pharmaceutical industry or CRO

  • Ability to advise and lead communication projects.

  • Understand drug development and communication process from development, launch through life cycle management.

  • In-depth knowledge of the technical and regulatory requirements related to the role.

  • Ability to advise and lead communication projects.

  • Understand drug development and communication process from development, launch through life cycle management.

  • In-depth knowledge of the technical and regulatory requirements related to the role.

Desirable Skills/Experience:

  • Advanced degree in a scientific discipline (Ph.D.)

This is a Hybrid role - minimum requirment 3 days per week onsite


When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

AstraZeneca is where innovation meets collaboration. We harness diverse knowledge to move with agility, working seamlessly across functions globally. Our team is empowered to make quick decisions, influencing drug development strategy at all levels. With a science-driven approach, we bring life-changing medicines to patients, constantly asking questions and trying new things. Your professional growth is passionately supported here, with opportunities to work on projects at all stages of development.

Ready to make an impact? Apply now and be part of our dynamic team!

The annual base pay (or hourly rate of compensation) for this position ranges from $133,042.40 - $199,563.60 USD Annual. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

10-Aug-2026

Closing Date

31-Aug-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

What AstraZeneca employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply